chr1:114356433:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr1:114,356,433-114,414,375
hg38 chr1:113,813,811-113,871,753 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.003 Cardiovascular Diseases NA BeFree,GAD Detail
0.008 celiac disease NA BeFree,GAD Detail
0.002 Cholangitis, Sclerosing NA GAD Detail
0.002 Chromosome Aberrations NA GAD Detail
<0.001 Churg-Strauss syndrome NA BeFree Detail
<0.001 colitis NA BeFree Detail
0.003 Connective Tissue Diseases NA BeFree,GAD Detail
0.154 Crohn Disease After Bonferroni correction for multiple testing, both the homozygous and the he... BeFree,GAD,GWASCAT 24971461 Detail
<0.001 dermatitis NA BeFree Detail
<0.001 dermatomyositis NA BeFree Detail
0.002 Diabetes INS,UBASH3A, and IFIH1 were significantly associated with progression from IA to... BeFree 25075402 Detail
0.004 diabetes mellitus INS,UBASH3A, and IFIH1 were significantly associated with progression from IA to... BeFree,GAD 25075402 Detail
0.013 Diabetes Mellitus, Non-Insulin-Dependent The frequency of PTPN22 polymorphisms in the MODY patients was similar to those ... BeFree,GAD 25896041 Detail
0.014 endometriosis NA BeFree,GAD,LHGDN Detail
0.003 Esophageal Achalasia NA BeFree,GAD Detail
<0.001 Disorder of eye NA BeFree Detail
0.002 Fetal Diseases NA GAD Detail
0.120 IgA glomerulonephritis NA CTD_human Detail
0.145 Graves Disease Association analyses were performed for genes with a known influence on developm... BeFree,CTD_human,GAD,LHGDN 25061884 Detail
0.002 Hemophilia A NA GAD Detail
0.005 hepatitis C NA BeFree,GAD,LHGDN Detail
<0.001 HIV Infections NA BeFree Detail
0.005 Hypertensive disease NA GAD Detail
<0.001 hyperthyroidism NA BeFree Detail
0.005 hypoparathyroidism NA GAD,LHGDN Detail
<0.001 hypothyroidism NA BeFree Detail
<0.001 Immune System Diseases NA BeFree Detail
0.005 Inflammation NA GAD Detail
0.129 Inflammatory Bowel Diseases Polymorphisms in the inflammatory pathway genes TLR2, TLR4, TLR9, LY96, NFKBIA, ... BeFree,CTD_human,GAD 24971461 Detail
0.145 Graves Disease We genotyped the five SNPs (rs12760457, rs2797415, rs1310182, rs2476599, and rs3... BeFree 20615141 Detail
0.001 thyroiditis We genotyped the five SNPs (rs12760457, rs2797415, rs1310182, rs2476599, and rs3... BeFree 20615141 Detail
<0.001 Kidney Diseases NA BeFree Detail
0.002 Kidney Failure, Chronic NA GAD Detail
<0.001 Fibroid Tumor Considering the whole sample, a borderline association between PTPN22 and leiomy... BeFree 25541531 Detail
0.002 leprosy NA GAD Detail
<0.001 chronic lymphocytic leukemia NA BeFree Detail
0.003 Biliary cirrhosis NA LHGDN Detail
0.003 Lupus Vulgaris Our objectives were to identify novel alternatively spliced forms of PTPN22 and ... BeFree,GAD 24433447 Detail
0.003 Lupus Erythematosus, Discoid Our objectives were to identify novel alternatively spliced forms of PTPN22 and ... BeFree,GAD 24433447 Detail
0.002 melanoma NA GAD Detail
0.002 Meniere disease NA GAD Detail
0.006 multiple sclerosis NA BeFree,GAD Detail
0.002 Musculoskeletal Diseases NA GAD Detail
<0.001 Mycoses NA BeFree Detail
0.002 myositis NA GAD Detail
0.524 rheumatoid arthritis Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheum... BeFree 23350658 Detail
<0.001 neuromyelitis optica NA BeFree Detail
<0.001 pemphigus vulgaris NA BeFree Detail
<0.001 plague NA BeFree Detail
<0.001 polymyalgia rheumatica NA BeFree Detail
0.002 Postoperative Complications NA GAD Detail
0.002 Pregnancy Complications, Hematologic NA GAD Detail
0.002 Prostatic Neoplasms NA GAD Detail
0.012 psoriasis PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasi... BeFree,GAD,LHGDN 25923216 Detail
0.003 purpura NA LHGDN Detail
<0.001 Henoch-Schoenlein purpura NA BeFree Detail
<0.001 rhabdomyosarcoma NA BeFree Detail
0.005 Rheumatism NA BeFree,GAD Detail
<0.001 rheumatic heart disease Influence of protein tyrosine phosphatase gene (PTPN22) polymorphisms on rheumat... BeFree 25273327 Detail
0.010 systemic scleroderma NA BeFree,GAD,LHGDN Detail
0.002 Dermatologic disorders NA GAD Detail
0.001 ankylosing spondylitis Association of PTPN22 polymorphsims and ankylosing spondylitis susceptibility. BeFree 25755798 Detail
<0.001 Cerebrovascular accident NA BeFree Detail
<0.001 synovitis NA BeFree Detail
0.002 Takayasu Arteritis NA GAD Detail
0.002 thrombocytopenia NA GAD Detail
0.008 Thyroid Diseases NA BeFree,GAD,LHGDN Detail
0.001 thyroiditis NA BeFree Detail
0.006 tuberculosis NA BeFree,GAD,LHGDN Detail
0.003 Tuberculosis, Pulmonary NA BeFree,GAD Detail
0.003 Turner syndrome NA BeFree,GAD Detail
<0.001 Uterine Fibroids PTPN22 and uterine leiomyomas. BeFree 25541531 Detail
0.003 anterior uveitis NA BeFree,GAD Detail
0.003 Uveomeningoencephalitic Syndrome NA BeFree,GAD Detail
<0.001 vasculitis NA BeFree Detail
0.136 vitiligo NA BeFree,GAD,GWASCAT,LHGDN Detail
<0.001 palindromic rheumatism NA BeFree Detail
0.005 Premature Birth NA GAD Detail
0.002 retinal vasculitis NA GAD Detail
<0.001 allergic asthma NA BeFree Detail
0.005 Autoimmune thyroid disease NA BeFree,GAD Detail
0.001 Diabetes, Autoimmune The absence of autoimmunity-associated PTPN22 alleles was also demonstrated in l... BeFree 25896041 Detail
<0.001 Adult type dermatomyositis NA BeFree Detail
0.002 age related macular degeneration NA GAD Detail
0.002 Gonadal Dysgenesis, 45,X NA GAD Detail
0.002 Disease Progression NA GAD Detail
0.003 Psoriasis vulgaris NA BeFree,GAD Detail
<0.001 Superficial ulcer NA BeFree Detail
<0.001 Maturity onset diabetes mellitus in young The frequency of PTPN22 polymorphisms in the MODY patients was similar to those ... BeFree 25896041 Detail
<0.001 Microscopic Polyangiitis NA BeFree Detail
0.002 prediabetes syndrome NA GAD Detail
<0.001 Hematologic Neoplasms NA BeFree Detail
<0.001 Polyradiculoneuropathy, Chronic Inflammatory Demyelinating NA BeFree Detail
0.003 Immune thrombocytopenic purpura NA BeFree,GAD Detail
0.027 lupus erythematosus Our objectives were to identify novel alternatively spliced forms of PTPN22 and ... BeFree,GAD 24433447 Detail
<0.001 Secondary antiphospholipid syndrome Significant association of the PTPN22 T1858 allele (CT + TT vs.CC) and secondary... BeFree 24985973 Detail
<0.001 Granulomatosis NA BeFree Detail
0.005 Hashimoto Disease NA BeFree,GAD Detail
<0.001 breast carcinoma NA BeFree Detail
0.001 Acute anterior uveitis NA BeFree Detail
<0.001 Idiopathic Inflammatory Myopathies NA BeFree Detail
<0.001 Endothelial dysfunction NA BeFree Detail
<0.001 Acute GVH disease NA BeFree Detail
0.008 autoimmune thyroiditis NA BeFree,GAD Detail
<0.001 Acute coronary syndrome Increased PTPN22 expression and defective CREB activation impair regulatory T-ce... BeFree 25814225 Detail
<0.001 Chronic inflammatory disorder NA BeFree Detail
0.001 Generalized vitiligo NA BeFree Detail
0.002 Sjogren's syndrome NA GAD Detail
<0.001 Non-ST elevation (NSTEMI) myocardial infarction Restoring CREB activity and silencing PTPN22 enhanced NSTEMI patients' ability t... BeFree 25814225 Detail
<0.001 Inflammatory polyarthritis NA BeFree Detail
0.001 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) NA BeFree Detail
0.003 coronary artery disease NA BeFree,GAD Detail
0.120 temporal arteritis NA ORPHANET Detail
<0.001 liver carcinoma NA BeFree Detail
0.003 Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis NA BeFree,GAD Detail
0.005 Chronic ulcerative colitis NA GAD Detail
0.120 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 NA UNIPROT Detail
0.005 granulomatosis with polyangiitis NA GAD,LHGDN Detail
0.005 Infection NA GAD,LHGDN Detail
0.002 Thymus Neoplasms NA GAD Detail
0.012 Addison Disease NA GAD,LHGDN Detail
0.009 alopecia areata NA BeFree,GAD,LHGDN Detail
<0.001 Alzheimer's disease NA BeFree Detail
<0.001 Anemia, Pernicious NA BeFree Detail
0.001 arteriosclerosis NA BeFree Detail
0.009 arthritis NA BeFree,GAD,LHGDN Detail
0.009 Arthritis, Psoriatic PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasi... BeFree,GAD,LHGDN 25923216 Detail
0.524 rheumatoid arthritis ORs for associations with different HLA-DRB1 alleles, PTPN22 genotypes and smoki... BeFree,CTD_human,GAD,GWASCAT,LHGDN,UNIPROT 24812286 Detail
0.524 rheumatoid arthritis Non-HLA genes PTPN22, CDK6 and PADI4 are associated with specific autoantibodies... BeFree,CTD_human,GAD,GWASCAT,LHGDN,UNIPROT 25138370 Detail
0.524 rheumatoid arthritis A C-to-T single-nucleotide polymorphism (SNP) located at position 1858 of human ... BeFree,CTD_human,GAD,GWASCAT,LHGDN,UNIPROT 26019128 Detail
0.003 atherosclerosis NA BeFree,GAD Detail
0.003 Bacterial Infections NA BeFree,GAD Detail
0.011 Behcet Syndrome NA BeFree,GAD,LHGDN Detail
<0.001 Malignant neoplasm of breast NA BeFree Detail
0.003 brucellosis NA BeFree,GAD Detail
0.003 Candidiasis, Chronic Mucocutaneous NA LHGDN Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
After Bonferroni correction for multiple testing, both the homozygous and the heterozygous variant g... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
INS,UBASH3A, and IFIH1 were significantly associated with progression from IA to diabetes (HR=1.65, ... DisGeNET Detail
INS,UBASH3A, and IFIH1 were significantly associated with progression from IA to diabetes (HR=1.65, ... DisGeNET Detail
The frequency of PTPN22 polymorphisms in the MODY patients was similar to those in geographically ma... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Association analyses were performed for genes with a known influence on development of GD - TSHR, HL... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Polymorphisms in the inflammatory pathway genes TLR2, TLR4, TLR9, LY96, NFKBIA, NFKB1, TNFA, TNFRSF1... DisGeNET Detail
We genotyped the five SNPs (rs12760457, rs2797415, rs1310182, rs2476599, and rs3789604) of the PTPN2... DisGeNET Detail
We genotyped the five SNPs (rs12760457, rs2797415, rs1310182, rs2476599, and rs3789604) of the PTPN2... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Considering the whole sample, a borderline association between PTPN22 and leiomyomas was observed: t... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Our objectives were to identify novel alternatively spliced forms of PTPN22 and to examine the expre... DisGeNET Detail
Our objectives were to identify novel alternatively spliced forms of PTPN22 and to examine the expre... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheumatoid arthritis in Z... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a fu... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Influence of protein tyrosine phosphatase gene (PTPN22) polymorphisms on rheumatic heart disease sus... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Association of PTPN22 polymorphsims and ankylosing spondylitis susceptibility. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
PTPN22 and uterine leiomyomas. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
The absence of autoimmunity-associated PTPN22 alleles was also demonstrated in latent autoimmune dia... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
The frequency of PTPN22 polymorphisms in the MODY patients was similar to those in geographically ma... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Our objectives were to identify novel alternatively spliced forms of PTPN22 and to examine the expre... DisGeNET Detail
Significant association of the PTPN22 T1858 allele (CT + TT vs.CC) and secondary antiphospholipid sy... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Increased PTPN22 expression and defective CREB activation impair regulatory T-cell differentiation i... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Restoring CREB activity and silencing PTPN22 enhanced NSTEMI patients' ability to generate Treg. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a fu... DisGeNET Detail
ORs for associations with different HLA-DRB1 alleles, PTPN22 genotypes and smoking were calculated s... DisGeNET Detail
Non-HLA genes PTPN22, CDK6 and PADI4 are associated with specific autoantibodies in HLA-defined subg... DisGeNET Detail
A C-to-T single-nucleotide polymorphism (SNP) located at position 1858 of human protein tyrosine pho... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs17337023 dbSNP
Genome
hg19
Position
chr1:114,356,433-114,414,375
Variant Type
snv
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